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- NP261345.RA74EYFF_gs56ufoeCrQ-zQDejlEYE3DJsRxCN7batJbw130_assertion type Assertion NP261345.RA74EYFF_gs56ufoeCrQ-zQDejlEYE3DJsRxCN7batJbw130_head.
- NP261345.RA74EYFF_gs56ufoeCrQ-zQDejlEYE3DJsRxCN7batJbw130_assertion description "[Mutations in KVLQT1 and KCNE1 also cause the Jervell and Lange-Nielsen syndrome, a form of LQTS associated with deafness, a phenotypic abnormality inherited in an autosomal recessive fashion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261345.RA74EYFF_gs56ufoeCrQ-zQDejlEYE3DJsRxCN7batJbw130_provenance.
- NP261345.RA74EYFF_gs56ufoeCrQ-zQDejlEYE3DJsRxCN7batJbw130_assertion evidence source_evidence_literature NP261345.RA74EYFF_gs56ufoeCrQ-zQDejlEYE3DJsRxCN7batJbw130_provenance.
- NP261345.RA74EYFF_gs56ufoeCrQ-zQDejlEYE3DJsRxCN7batJbw130_assertion SIO_000772 10973849 NP261345.RA74EYFF_gs56ufoeCrQ-zQDejlEYE3DJsRxCN7batJbw130_provenance.
- NP261345.RA74EYFF_gs56ufoeCrQ-zQDejlEYE3DJsRxCN7batJbw130_assertion wasDerivedFrom befree-20140225 NP261345.RA74EYFF_gs56ufoeCrQ-zQDejlEYE3DJsRxCN7batJbw130_provenance.
- NP261345.RA74EYFF_gs56ufoeCrQ-zQDejlEYE3DJsRxCN7batJbw130_assertion wasGeneratedBy ECO_0000203 NP261345.RA74EYFF_gs56ufoeCrQ-zQDejlEYE3DJsRxCN7batJbw130_provenance.